QC Analyst Role:
Testing may include, but is not limited to, routine particle size analysis (laser diffraction), cleaning verification (HPLC), identification testing (FTIR/ Raman), method development and validation, differential scanning calorimetry (DSC), Method optimisation and trouble-shooting, technology transfer and pharmacopoeia analyses as appropriate.
Perform analytical testing in an accurate, timely and efficient manner, consistent with cGMP requirements.
Ensure documentation is accurate, legible and presented clearly and concisely, consistent with cGMP requirements.
Prepare analytical test methods.
Environmental Monitoring and periodically microbiological testing.
Prepare analytical reports: Laboratory Investigation, Statement of Results and Certificate of Analysis.

Your Background:
A Levels in science or higher
HPLC experience advantageous
Excellent communication skills
IT literate (Microsoft Office: Word, Excel, Power Point)
Experience within a GMP environment is desirable

Apply:
For more information, or to apply for this QC Analyst position please contact the Key Accounts Team on 01438 870011 or email pharmacontracts@ckagroup.co.uk. Please quote reference 53156.